CA1192462A

CA1192462A - Epistaxis sponge

Info

Publication number: CA1192462A
Application number: CA000415128A
Authority: CA
Inventors: Avvari Rangaswamy
Original assignee: Individual
Current assignee: Individual
Priority date: 1982-01-27
Filing date: 1982-11-08
Publication date: 1985-08-27
Also published as: JPS58133252A; ATE23261T1; DE3367322D1; EP0084960B1; EP0084960A1

Abstract

ABSTRACT OF THE DISCLOSURE
An article to be used as an aid in the treat-ment of epistaxis containing a fluid absorbing portion shaped for approximate adaptation into at least part of the nasal cavity and containing a semi-rigid handle portion anchored within the fluid absorbing portion and extending a sufficient dis-tance beyond the fluid absorbing portion to be capable of being readily grasped by a use to enable the manipulation of the fluid absorbing portion into and out of the nasal cavity during the treatment of epistaxis.

Description

62, TITLE: EPIST~YIS SPONGE

BACKGROUND OF THE INVENTION
Epis~axis or nose bleed while quite common and generally experienced by everyone at one time or another is at best an inconvenient and often disturb-ing experience. Even though considerable advanceshave been achieved in the treatment of a wide ~ariety of disorders, the time honored methods for controlling anterior nose bleeds remain rela~ively unimproved.
Simply tilting the head back, using cold compresses, squeezing the anterior part of~the nose, i.e. the sep-tum, and finally packing the nasal cavity are employed as standard epistaxis inhibiting techniques. The drawbacks to these techniques are personally known to almost everyone and in particular the discomfort of squeezing the nose with the resultant need for breathing through the mouth. In the case of packing, there is a need for special instruments and profes-sional expertise when both packing and unpacking the nasal cavity.
Nose bleeds can occur for a wide variety of reasons including rheumatic fever, infectious mono-nucleosis~ sickel cell anemia, systemic haemorrhagic disorders and hypertension (in adults), hemangiomas, hereditary telangiectasis and an~lo:Eibromas. The most common cause ol- epistaxis in ~hildren arise in the nasal cavity, for example, by excessive drying, w~ich can be traumatized ~y such activities as nose picking. The most common location for such varicosities is on the nasal septum above the nasal floor and approximately 0.5 cm inside the nose. This is characterized as Kiesselbauch's area and is the anastomotic site for a number of arterioles.
Traumatizin~ a varicosity in this area sufficiently to produce epistaxis is commonly referred to as an anterior nose bleed.
SUMMARY OF THE INVENTION
A shaped, semi-rigid and absorbent device is provided which is adapted to be easily inserted and removed from the nasal cavity. Such a shaped devlce is by virtue of its structure capable of absorbing ~he blood while providing pressure on the traumatized mucosa, which will tend to inhibit further bleedina.
An aspect of this invention is as follows:
An epistaxis treatment device comprising a handle means for inserting into, and removing from, a nasal cavity a fluid absorbing pad having a longitudinal axis essentially parallel to the longitudinal axis of said handle means;

-2a-perpendicular to said longi-tudinal axis of said fluid absorb-ing pad the outside shape of said fluid absorbing pad is substantially pear shaped in cross section; the height of said pear shaped cross section being about twice the maximum width, and the axis of said maximum width being positioned at a location o~her than at the middle of the height axis;
whereby insertion of said pear shaped fluid absorbing pad in a nasal cavity facilitates absorption of fluid and applies pressure on the traumatized mucosa of the nasal cavity.

BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a perspective view of the device of the present invention.
Fig. 2 is an end view from the direction shown by the arrow I of Fig. 1.

2~

Fig. 3 is a partial cross sectional view taken along the lines and arrows 3-3 in Fig. 1.
DETAILED DESCRIPTION OF THE DRAWINGS
The device of the presQnt invention is charac-teristically constructed around a semi-rigid, flexible stem 1 which is provided with a gripping portion or handle 2 and an anchor 3. The length of the stem can vary as well as the specific shape of the handle and the configuration of the anchor depending on the functional requirements and physical properties of the materials selected. Of importance, is the requirement that the stem 1 be both rigid and yet flexible enough for manipulation during insertion of the shaped ab-sorbent tip into the nasal cavity and removal there-from while providing some support for the remainderof the structure. In the embodiment shown, a thin wire stem is provided which provides the necessary functionality when absorbent cotton 4 is utilized as the core material surrounded with at least one and preferably more than one cotton gauze outer wrapping 5.
It is of course possible to substitute sultable plastic materials for the metal stem. Likewise, different handle and anchoring configurations can be ,L4~

employed wl~hout the need for extensive experimen-tation. The co~ton gauze and absorbent cotton may also be replaced with suitable natural or syn~hetic-ally manufactured absorbent materials as long as the finished device retains the capacity to generally hold its shape and preferably expand slightly when absorbing blood through the outer surface and into the interior of the device.
In the embodiment shown, conventional absorbent cotton 4 is provided as the core supported by the metal stem 1 and its associated anchor 3 and surround-ed typically by several layers of cotton gau2e 5 to form generally the shape shown in Figs. 1 and 2.
For optimum results, the dimension a-b ~Fig. 3) should be approximately 4 cm to be suitable for an adult. Several sizes can, of ccurse, be constructed, i.e. 3.5 cm, 3 cm and 2c, to accommodate differences in patient anatomy. The most preferred dimensions will approximately bear the following relative rela-tionships in the embodiment described:
Length Height Width a-b 4 cm c-d 2.5 cm e-f 1.25 cm

3-5 cm 2.25 cm 1.125 cm 3.0 cm 2.0 cm 1.0 cm 2.0 cm 1.5 cm 0.75 cm V ~

The anteroposterior dimension (c-d3 and the transverse dimension (e-f) are important for both adaptation and a comfortable fit for the device into ~he nasal cavity. It is a particularly important aspect of the present invention ~hat the pear-shaped cross section be maintained as close as is practical to the pear-like shape of the vestibule of the an-terior nasal cavity. In general, a width (c-~), measured laterally or transversely of the width at a point below the mid-point of the cross-section shown in Fig. 2, would preferably be approximately one-half the height (c-d) of the article.
- The expistaxis 5ponge of the present invention can also be used to sponge or mop or provide control of bleeding points in the mucosa of the nasal cavity during minor surgery.
This invention has been described with reference to its current preferred embodiment, however, it will be appreciated that a wide variation in material selection is possible and other materials may be sub-stituted and obtain the functional aclvantages dis-closed herein. Likewise, further modifications are possible, as for example, the incorporation of soluble m~dicaments in the absorbent material or on the sur-face thereof to aid on coagulation, the prevention of --6--infection or ~he like, withou~ detracting fro~ the funetion of the device, where such additives are a contempla~ed improvement for either a general or specialized function.

~,,

Claims

WHAT IS CLAIMED IS:

1. An epistaxis treatment device comprising a handle means for inserting into, and removing from, a nasal cavity a fluid absorbing pad having a longitudinal axis essentially parallel to the longitudinal axis of said handle means;
perpendicular to said longitudinal axis of said fluid absorb-ing pad the outside shape of said fluid absorbing pad is substantially pear shaped in cross section; the height of said pear shaped cross section being about twice the maximum width, and the axis of said maximum width being positioned at a location other than at the middle of the height axis, whereby insertion of said pear shaped fluid absorbing pad in a nasal cavity facilitates absorption of fluid and applies pressure on the traumatized mucosa of the nasal cavity.

2. The epistaxis treatment device as set forth in Claim 1 in which said fluid absorbing pad is affixed to said handle means, and said handle means extends beyond the end of said fluid absorbing pad a sufficient distance to be capable of being grasped for positioning and inserting said fluid absorbing pad in a nasal cavity thereby providing for ease of insertion of said fluid absorbing pad into the nasal cavity and subsequent removal therefrom.

3. The epistaxis treatment device as set forth in Claim 1 in which a core of absorbent cotton is surrounded by at least one layer of cotton gauze to form said fluid absorbent pad.

4. The epistaxis treatment device as set forth in Claim 1 in which fluid absorbing materials capable of resil-iently expanding when absorbing fluid are used to form said fluid absorbing pad, thereby increasing the pressure applied by said fluid absorbing pad to the nasal mucusa as fluid is absorbed.